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Mireia Vilardell

Showing results (1-10 of 22) with videos related to

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Bioinformatics (Oxford, England)|October 27, 2006
Hypothesis testing approaches to the exon prediction problemMireia Vilardell, Alex Sánchez-Pla
Biology Open|August 17, 2013
An integrative computational analysis provides evidence for FBN1-associated network deregulation in trisomy 21Mireia Vilardell, Sergi Civit, Ralf Herwig
Biomed Research International|October 15, 2014
WISCOD: a statistical web-enabled tool for the identification of significant protein coding regionsMireia Vilardell, Genis Parra, Sergi Civit
Human Genetics|April 20, 2010
Transcriptome profile in Williams-Beuren syndrome lymphoblast cells reveals gene pathways implicated in glucose intolerance and visuospatial construction deficitsAnna Antonell, Mireia Vilardell, Luis A Pérez Jurado
Advances in Experimental Medicine and Biology|September 28, 2016
Validation of Transcriptomics-Based In Vitro MethodsRaffaella Corvi, Mireia Vilardell, Jiri Aubrecht, et al.
BMC Genomics|May 17, 2011
Meta-analysis of heterogeneous Down Syndrome data reveals consistent genome-wide dosage effects related to neurological processesMireia Vilardell, Axel Rasche, Anja Thormann, et al.
BMC Medical Genetics|April 15, 2008
Array-CGH in patients with Kabuki-like phenotype: identification of two patients with complex rearrangements including 2q37 deletions and no other recurrent aberrationIvon Cuscó, Miguel del Campo, Mireia Vilardell, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 17, 2007
Study of candidate genes affecting the progression of renal disease in autosomal dominant polycystic kidney disease type 1Bárbara Tazón-Vega, Mireia Vilardell, Laureano Pérez-Oller, et al.
Human Molecular Genetics|February 28, 2009
Autism-specific copy number variants further implicate the phosphatidylinositol signaling pathway and the glutamatergic synapse in the etiology of the disorderIvon Cuscó, Andrés Medrano, Blanca Gener, et al.
Gaceta Sanitaria|December 22, 2018
[Excess mortality among breast cancer patients in early stages in Tarragona and Gerona (Spain)]Ramon Clèries, Alberto Ameijide, Maria Buxó, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Bioinformatics (Oxford, England)|October 27, 2006
Hypothesis testing approaches to the exon prediction problemMireia Vilardell, Alex Sánchez-Pla
Biology Open|August 17, 2013
An integrative computational analysis provides evidence for FBN1-associated network deregulation in trisomy 21Mireia Vilardell, Sergi Civit, Ralf Herwig
Biomed Research International|October 15, 2014
WISCOD: a statistical web-enabled tool for the identification of significant protein coding regionsMireia Vilardell, Genis Parra, Sergi Civit
Human Genetics|April 20, 2010
Transcriptome profile in Williams-Beuren syndrome lymphoblast cells reveals gene pathways implicated in glucose intolerance and visuospatial construction deficitsAnna Antonell, Mireia Vilardell, Luis A Pérez Jurado
Advances in Experimental Medicine and Biology|September 28, 2016
Validation of Transcriptomics-Based In Vitro MethodsRaffaella Corvi, Mireia Vilardell, Jiri Aubrecht, et al.
BMC Genomics|May 17, 2011
Meta-analysis of heterogeneous Down Syndrome data reveals consistent genome-wide dosage effects related to neurological processesMireia Vilardell, Axel Rasche, Anja Thormann, et al.
BMC Medical Genetics|April 15, 2008
Array-CGH in patients with Kabuki-like phenotype: identification of two patients with complex rearrangements including 2q37 deletions and no other recurrent aberrationIvon Cuscó, Miguel del Campo, Mireia Vilardell, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 17, 2007
Study of candidate genes affecting the progression of renal disease in autosomal dominant polycystic kidney disease type 1Bárbara Tazón-Vega, Mireia Vilardell, Laureano Pérez-Oller, et al.
Human Molecular Genetics|February 28, 2009
Autism-specific copy number variants further implicate the phosphatidylinositol signaling pathway and the glutamatergic synapse in the etiology of the disorderIvon Cuscó, Andrés Medrano, Blanca Gener, et al.
Gaceta Sanitaria|December 22, 2018
[Excess mortality among breast cancer patients in early stages in Tarragona and Gerona (Spain)]Ramon Clèries, Alberto Ameijide, Maria Buxó, et al.
Pageof 3